Canonical Allele Identifier: CA403493842
Gene: KDM4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5071042T>C , CM000681.2:g.5071042T>C GRCh38
NC_000019.9:g.5071053T>C , CM000681.1:g.5071053T>C GRCh37
NC_000019.8:g.5022053T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000159111.9:c.659T>C MANE Select ENSP00000159111.3:p.Leu220Pro
ENST00000159111.8:c.659T>C ENSP00000159111.3:p.Leu220Pro
ENST00000381759.8:c.659T>C ENSP00000371178.3:p.Leu220Pro
ENST00000536461.5:c.659T>C ENSP00000440495.1:p.Leu220Pro
ENST00000589104.5:n.425T>C
ENST00000592175.5:n.370T>C
ENST00000611640.4:c.659T>C ENSP00000480642.1:p.Leu220Pro
NM_015015.2:c.659T>C NP_055830.1:p.Leu220Pro
XM_005259521.2:c.659T>C XP_005259578.2:p.Leu220Pro
XM_011527814.1:c.383T>C XP_011526116.1:p.Leu128Pro
XM_011527815.1:c.659T>C XP_011526117.1:p.Leu220Pro
XM_011527818.1:c.659T>C XP_011526120.1:p.Leu220Pro
XM_011527819.1:c.659T>C XP_011526121.1:p.Leu220Pro
XM_011527820.1:c.659T>C XP_011526122.1:p.Leu220Pro
XM_011527821.1:c.659T>C XP_011526123.1:p.Leu220Pro
XM_011527822.1:c.659T>C XP_011526124.1:p.Leu220Pro
XR_936167.1:n.854-6325T>C
XM_005259521.4:c.659T>C XP_005259578.2:p.Leu220Pro
XM_011527814.2:c.383T>C XP_011526116.1:p.Leu128Pro
XM_011527818.3:c.659T>C XP_011526120.1:p.Leu220Pro
XM_011527819.2:c.659T>C XP_011526121.1:p.Leu220Pro
XM_011527820.2:c.659T>C XP_011526122.1:p.Leu220Pro
XM_011527821.2:c.659T>C XP_011526123.1:p.Leu220Pro
XM_011527822.2:c.659T>C XP_011526124.1:p.Leu220Pro
XM_017026503.1:c.659T>C XP_016881992.1:p.Leu220Pro
XM_017026504.2:c.659T>C XP_016881993.1:p.Leu220Pro
XM_017026505.2:c.659T>C XP_016881994.1:p.Leu220Pro
XR_936167.2:n.879-6325T>C
NM_015015.3:c.659T>C MANE Select NP_055830.1:p.Leu220Pro
NM_001370093.1:c.659T>C NP_001357022.1:p.Leu220Pro
NM_001370094.1:c.659T>C NP_001357023.1:p.Leu220Pro